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Renuvion® APR Handpiece

Page Type
Cleared 510(K)
510(k) Number
K223262
510(k) Type
Traditional
Applicant
Apyx Medical Corporation
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/23/2023
Days to Decision
122 days
Submission Type
Summary

Renuvion® APR Handpiece

Page Type
Cleared 510(K)
510(k) Number
K223262
510(k) Type
Traditional
Applicant
Apyx Medical Corporation
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/23/2023
Days to Decision
122 days
Submission Type
Summary